The rates of hydrodechlorination catalyzed by Pd supported on carbon for four chlorofluorocarbons spanned a range of 7 orders of magnitude. The rates scaled up to the bond strength of the carbon−chlorine bond for the gas-phase reactant. This finding demonstrates that the rate-determining step involves the scission of the C−Cl bond and suggests, through Polanyi and linear free-energy relationships, that rates for other compounds can be estimated if the C−Cl bond strength is known. The reaction orders for the most abundant products are approximately first-order for the chlorine-containing compound, half-order in H2, and inverse first-order in HCl. The reaction steps consistent with these orders include a rate-determining step involving the adsorption of the chlorofluorocarbon to a single site (which could be a single surface palladium atom) and equilibrated steps between gas-phase H2, gas-phase HCl, and adsorbed hydrogen and chlorine atoms. The rates on the supported catalysts are comparable to the ones reported before on a Pd foil, indicating that the support does not play a role in the reaction. The product distribution is independent of conversion, implying that the various products are formed from a single visit of the reactant on the surface and not from readsorption of gas-phase products. The four compounds studied were chloropentafluoroethane (CF3−CF2Cl), 2-chloro-1,1,1,2-tetrafluoroethane (CF3−CFClH), 1,1-dichlorotetrafluoroethane (CF3−CFCl2), and 1,1,1-trichloro-2,2,2-trifluoroethane (CF3−CCl3).

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